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EC number: 219-786-3 | CAS number: 2530-86-1
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Short-term toxicity to aquatic invertebrates
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2017-03-27 to 2017-08-03
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: OECD Guideline; EU Method; GLP
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 017
- Report date:
- 2017
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Series on Testing and Assessment, No. 23, "Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures"
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- N,N-dimethyl-3-(trimethoxysilyl)propylamine
- EC Number:
- 219-786-3
- EC Name:
- N,N-dimethyl-3-(trimethoxysilyl)propylamine
- Cas Number:
- 2530-86-1
- Molecular formula:
- C8H21NO3Si
- IUPAC Name:
- dimethyl[3-(trimethoxysilyl)propyl]amine
- Test material form:
- liquid
- Details on test material:
- - Name (as cited in the report): SAT 170001
- Chemical Name: N,N-dimethyl-3-(trimethoxysilyl)propylamine
- CAS No.: 2530-86-1
- Batch No.: 186020160504
- Aggregate State at RT: liquid
- Colour: colourless
- Storage Conditions: room temperature
- Expiry Date: 30.08.2017
Constituent 1
- Specific details on test material used for the study:
- Name: N,N-Dimethyl-3-(trimethoxysilyl)propylamine
CAS No.: 2530-86-1
EC-No.: 219-786-3
Batch No.: 186020160504
Purity: 99.4 %
according to final report (Study number: 16-11327)
Final Report Date
(Study Number: 16-11327) :
September 14, 2016
Aggregate State at Room Temperature: Liquid
Solubility Soluble in water at tested concentration
Stability Not stable in water, after 70min complete hydrolysis/condensation is observed (Study number: 16-17622-5). Most likely primary hydrolysis product is N,N-Dimethyl-3-(trihydroxysilyl)propylamine
Colour: Colourless
Expiry Date: August 30, 2017
Storage Conditions at Test Facility:
At 20 -/- 5 °C, in the dark
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- Duplicate samples from the freshly prepared test medium of the only test concentration and the control were taken at the start of the test.
For the determination of the TOC content of the test item and/or its hydrolysis products at the end of the test, duplicate samples from the test medium of the only test concentration and the control were collected at the end of the test (after 48 hours) by pooling the contents of the beakers of each treatment.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Test Concentration: The parent compound hydrolyses during the exposure period. According to stability studies in water (AB 16-17662-5) after 70 minutes complete hydrolysis/condensation is observed. Due to the very short half-life period, the test was conducted with the mixture of reaction products and the residues of N,N-Dimethyl-3-(trimethoxysilyl)propylamine that remain after stirring of 24 hours. The parent compound is likely to hydrolyse mainly to N,N-Dimethyl-3-(trihydroxysilyl)propylamine. Furthermore, condensation products and polymeric species may exist. Test results are based on nominal concentration.
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Species: Daphnia magna (Straus), clone 5
Age at Test Start: From 3.5 to 20.25 hours old
Sex: Female
Origin: The daphnids introduced in the test were taken from ibacon's in house laboratory culture.
Breeding Conditions: The daphnids were bred in the laboratories of ibacon under similar temperature and light conditions as used in the test. The cultivation of the parental daphnids was performed in Elendt M4 medium. The test organisms were not first brood progeny. The daphnids in the stock culture were fed at least on all working days with green algae (Desmodesmus subspicatus) freshly grown in the laboratories of ibacon.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- Water Hardness: 2.5 mmol/L (= 250 mg/L) as Calcium Carbonate
- Test temperature:
- 20.3 to 21.3 °C at test start;
20.0 to 20.1 °C at test end - pH:
- 8.4 to 8.6 at test start;
8.0 at test end; and thus the pH-value did not vary by more than 1.5 units - Dissolved oxygen:
- 6.0 to 8.8 mg/L at test start;
8.7 mg/L at test end - Nominal and measured concentrations:
- The parent compound hydrolyses during the exposure period. According to stability studies in water (AB 16-17662-5) after 70 minutes complete hydrolysis/condensation is observed. Due to the very short half-life period, the test was conducted with the mixture of reaction products and the residues of N,N-Dimethyl-3-(trimethoxysilyl)propylamine that remain after stirring of 24 hours. The parent compound is likely to hydrolyse mainly to N,N-Dimethyl-3-(trihydroxysilyl)propylamine. Furthermore, condensation products and polymeric species may exist. Test results are based on nominal concentration of 100.1 mg test item/L.
- Details on test conditions:
- Test Environment: Controlled environment room
Measurement of pH, Dissolved
Oxygen and Water Temperature:
The water temperature, pH-values and dissolved oxygen concentrations were determined at test start and test end in each treatment group.
Water Temperature: 20.3 to 21.3 °C at test start;
20.0 to 20.1 °C at test end
pH-Values: 8.4 to 8.6 at test start;
8.0 at test end; and thus the pH-value did not vary by more than 1.5 units
Dissolved Oxygen Concentration: 6.0 to 8.8 mg/L at test start;
8.7 mg/L at test end
Light Regime: 16 h light : 8 h dark
Light Intensity: The light intensity was 360 to 570 lux (measured once during the test). - Reference substance (positive control):
- yes
- Remarks:
- For the evaluation of the quality of the Daphnia clone and the consistency of the experimental conditions, the reference item potassium dichromate is tested at least twice a year to demonstrate satisfactory test conditions.
Results and discussion
Effect concentrationsopen allclose all
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 100.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- After 48 hours of exposure no immobilisation of the test animals was observed in the control and in the only test concentration of nominal 100.1 mg test item/L.
- Results with reference substance (positive control):
- In the most recent test with the reference item potassium dichromate performed in January 2017 the EC50 after 24 hours was determined to be 1.48 mg test item/L, indicating that the sensitivity of the daphnids was consistent with the level proposed by the OECD 202 guideline (EC50-24 h between 0.6 and 2.1 mg potassium dichromate/L).
- Reported statistics and error estimates:
- No statistical analysis was performed.
The EC50 could not be quantified due to the absence of toxicity of the test item. The NOEC and the LOEC were determined directly from the raw data.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Remarks:
- Control Immobilisation Rate was 0 % and furthermore no daphnid showed signs of disease or stress. Dissolved Oxygen Concentration was above or equal 8.7 mg O2/L in the control and test vessels at the end of the test.
- Conclusions:
- The toxic effect of the test item N,N-Dimethyl-3-(trimethoxysilyl)propylamine to Daphnia magna was assessed in a static limit test with its reaction products. The 48-hour NOEC was determined to be ≥ 100.1 mg test item/L. The 48-hour LOEC was determined to be > 100.1 mg test item/L and the 48-hour EC50 value was determined to be > 100.1 mg test item/L.
The quantification of the test item N,N-Dimethyl-3-(trimethoxysilyl)propylamine and / or its hydrolysis products in the test samples was performed by analysing the Total Organic Carbon content (TOC).
At the start of the test 101% of the nominal test concentration were found. After 48 hours test duration, 98% of the nominal value was determined. During the test the daphnids were exposed to a mean of 100% of nominal. Therefore, all reported results refer to nominal concentrations. - Executive summary:
Title: N,N-Dimethyl-3-(trimethoxysilyl)propylamine: Acute Toxicity to Daphnia magna in a Static 48-hour Immobilisation Limit Test
Purpose: The purpose of this study was to determine the influence of the test item N,N-Dimethyl-3-(trimethoxysilyl)propylamine on the mobility of Daphnia magna.
For this purpose, young daphnids (< 24 hours old) were exposed in a static test for 48 hours to the only concentration of nominal 100.1 mg/L under defined conditions for 48 hours. The recorded effects were the mobility of the daphnids after 24 and 48 hours. This limit-test was performed in compliance with the test guidelines in order to demonstrate that the test item has no toxic effects on the daphnids up to this concentration. The test method of application and the test system are recommended by the test guidelines and Daphnia magna is the recommended test species. The purpose of the analytical part of this study was to determine the content of total organic carbon (TOC) of the test item and/or its hydrolysis products in the test medium.
Guidelines:
Commission Regulation (EC) No 440/2008, Annex, Part C, C.2.: "Daphnia sp. Acute Immobilisation Test", Official Journal of the European Union (EN), dated May 30, 2008
OECD Guideline for Testing of Chemicals No. 202: "Daphnia sp., Acute Immobilisation Test" adopted April 13, 2004
OECD Series on Testing and Assessment, No. 23, "Guidance Document on Aquatic Toxicity Testing of Difficult Substances and Mixtures", December 15, 2000
SANCO/3029/99 rev.4 11/07/00: Residues: Guidance for generating and reporting methods of analysis in support of pre-registration data requirements for Annex II (part A; Section 4) and Annex III (part A; Section 5) of directive 91/414
Material and Methods
Test Item: N,N-Dimethyl-3-(trimethoxysilyl)propylamine; batch no.: 186020160504; purity: 99.4 %, according to certificate of analysis
Test Species: Female Daphnia magna, clone 5; 3.5 to 20.25 hours old
Source: The daphnids introduced in the test were taken from ibacon's in-house laboratory culture.
Test Design: This study encompassed two treatment groups (one test item concentration at nominal 100.1 mg/L, and one control) each containing 20 individuals. The mobility of the daphnids was determined in a static 48-hour test by visual observation after 24 and 48 hours.
Endpoints: Number of immobile organisms after 24 and 48 hours
Test Concentration: The parent compound hydrolyses during the exposure period. According to stability studies in water (AB 16-17662-5) after 70 minutes complete hydrolysis/condensation is observed. Due to the very short half-life period, the test was conducted with the mixture of reaction products and the residues of N,N-Dimethyl-3-(trimethoxysilyl)propylamine that remain after stirring of 24 hours. The parent compound is likely to hydrolyse mainly to N,N-Dimethyl-3-(trihydroxysilyl)propylamine. Furthermore, condensation products and polymeric species may exist. Test results are based on nominal concentration.
Test Conditions: Water temperature: 20.0 to 21.3 °C; pH value: 8.0 to 8.6; dissolved oxygen concentration: 6.0 to 8.8 mg/L; photoperiod: 16 h light - 8 h dark; light intensity: 360 to 570 lux; and thus were within the ranges requested by guideline OECD 202
Results
Biological test results: After 48 hours of exposure no immobilisation of the test animals was observed in the control and in the only test concentration of nominal 100.1 mg test item/L.
Conclusion:
The toxic effect of the test item N,N-Dimethyl-3-(trimethoxysilyl)propylamine to Daphnia magna was assessed in a static limit test with its reaction products. The 48-hour NOEC was determined to be ≥ 100.1 mg test item/L. The 48-hour LOEC was determined to be > 100.1 mg test item/L and the 48-hour EC50 value was determined to be > 100.1 mg test item/L. The quantification of the test item N,N-Dimethyl-3-(trimethoxysilyl)propylamine and / or its hydrolysis products in the test samples was performed by analysing the Total Organic Carbon content (TOC). At the start of the test 101% of the nominal test concentration were found. After 48 hours test duration, 98% of the nominal value was determined. During the test the daphnids were exposed to a mean of 100% of nominal. Therefore, all reported results refer to nominal concentrations.
This study is classified as acceptable and satisfies the guideline requirements for an acute toxicity study with freshwater invertebrates.
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